Feb 1 (Reuters) - Pharnext SA PHARN.PA :
* PROVIDES AN UPDATE ON ITS PIVOTAL CLINICAL DEVELOPMENT
PROGRAM
FOR ITS LEAD MEDICINE PXT3003 IN CHARCOT-MARIE-TOOTH TYPE 1A
('CMT1A')
* EXPECTS TO BEGIN FIRST-PATIENT-FIRST-DOSE IN ITS CLINICAL
PIVOTAL PHASE III TRIAL ENTITLED PREMIER BEFORE MARCH 31, 2021
IN U.S.
* PREMIER TRIAL IS EXPECTED TO ENROLL APPROXIMATELY 350
SUBJECTS
FROM 50 CENTERS WORLDWIDE
* PHARNEXT HAS ALSO APPLIED FOR, AND IS INTERACTING WITH FDA
REGARDING A SPECIAL PROTOCOL ASSESSMENT ('SPA') FOR PREMIER
PHASE III TRIAL
* PHARNEXT WILL BE REPORTING TOP-LINE INTERIM DATA ON SAFETY
AND
EFFICACY OF PXT3003 COLLECTED SO FAR FROM THIS OPEN LABEL STUDY
DURING Q2 2021
Source text for Eikon: ID:nEQ2PH4Ppa
Further company coverage: PHARN.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))